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COX-2 Inhibitor With Concurrent Chemoradiation in Locally Advanced Head & Neck Carcinoma

Phase 3
Conditions
Head and Neck Cancer
Interventions
Drug: placebo
Registration Number
NCT00603759
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

chemotherapy- and radiotherapy-induced oral mucositis represents a therapeutic challenge frequently encountered in cancer patients.This side effect causes significant morbidity and may delay or interrupt the treatment plan, as well reduce therapeutic index. cyclo-oxygenase 2 (COX-2) is an inducible enzyme primarily expressed in inflamed tissues and tumor. COX-2 inhibitors have shown promise as radio- and chemosensitizer and reduce radio-induced toxicities.

we have conducted a phase III, randomized double blind clinical trial to evaluate the toxicity and efficacy of celecoxib, a selective COX-2 inhibitor, administered concurrently with chemotherapy, and radiation for locally advanced head and neck cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
122
Inclusion Criteria
  • stage III/IV (locally advanced) carcinoma of oropharynx, oral cavity, hypopharynx, larynx, or nasopharynx
  • primary treatment with chemoradiation
Exclusion Criteria
  • distant metastasis
  • incomplete treatment
  • adjuvant chemoradiation after surgery without apparent tumor

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1celecoxib-
2placebo-
Primary Outcome Measures
NameTimeMethod
efficacy of celecoxib (response rate and local control)30 months
Secondary Outcome Measures
NameTimeMethod
toxicity of celecoxib30 months

Trial Locations

Locations (1)

Department of Chemoradiation

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Tehran, Iran, Islamic Republic of

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